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Lineages and Results of Y-DNA Testing for STRAUB, TRAUB, STRAUBE, STROOP, STRUB,
and Variations, especially STROUP, STROUPE, TROUP, TROUPE, etc.
Haplogroup I1-AS5 — STRAUB of Großgartach, Württemberg
Results
Hub
Y-DNA Haplogroups Represented in the Project
(number tested at FTDNA + number tested elsewhere / number of different progenitors)
Project
Home
E (1 / 1)  I1  (4 / 3) I1-AS5 (23 / 1)  I2  (5+1 / 4) J2 (4 / 2) R1a (2 / 1) R1b (14 / 12) T (1 / 1)

I1-AngloSaxon-5, a.k.a., I-M253-AS5
I1-AngloSaxon is the most common form of Haplogroup I1, which is the second most common haplogroup in western Europe, after R1b.  It is most frequent in the Netherlands, northwestern Germany, and Denmark and is present at lower frequencies in eastern and southern Germany, southern Sweden, and the British Isles.  The most common form of I1-AS is AS1.  AS5 is uncommon.

These I1-AS5 individuals are closely related.  None has less than a 62/67 match with each other, and none of those tested to 67 markers matches the modal haplotype at less than 64/67 markers.  They have rare haplotypes that are, at least for now, unique and easily distinguishable — beyond their matches with each other, they have no full matches with anyone else at 25 markers and no full or even near matches with anyone else at 37 or more markers. 

The big news here (20 Mar 2008) is the match of the American STRAUBs with the Württemberg STRAUB (#111298).  We have crossed the pond!  Our earliest known common ancestor is Martin STRAUB (1616-1676) of Gemmingen, then Grossgartach, in the Heilbronn District of Wuerttemberg, Germany.  Martin is the paternal grandfather of Johann Pieter STRAUB (1695- ), 1733 immigrant to Philadelphia and ancestor of President Barack OBAMA.  Anyone in the table below who does not descend directly from Martin at least descends from someone closely related to him.


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Red labels indicate markers that typically mutate more frequently than those labeled in black.
(Empty cells that are darkened indicate tests not ordered.)

To view the subject's lineage, please scroll to the right.
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Surname Kit # Ysearch
User ID
Haplotype— as determined by Family Tree DNA's "Standard" STR tests Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
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S1
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I1-AngloSaxon-5 modal values 14 22 14 10 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 20 28 12 14 15 15     10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 9 12 22 25 15 10 12 12 15 8 13 25 20 13 13 11 12 10 11 12 11 as per Nordtvedt
                 
0 STROUP 78741 H5K5T 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt11, Pvt10, Warren LeRoy9, Samuel Tilden8, Jacob7, Jonathan6, Joh. Adam5, Joh. Daniel4, Joh. Pieter I3, Hans Adam2, Martin1
STROUPE 94379   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt11, Pvt10, M.H.9, James Henderson8, Ephraim7, [David-or-Elias]6, Philip5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STROUP 145951   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8 9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt10, Pvt9, Sydney Shuford8, Malcolm Napoleon7, Levi6, Philip5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STROUPE 143321   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt11, Pvt10, Aaron Hubert9, Michael Luther8, John Michael7, Abner Albert6, Daniel5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
BELEW 97358 SYHF3 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, Pvt4, John Larkin3, Silas2, Solomon1 BELEWpresumed descendant of Andrew6, Adam5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STRAUB 26156 BUHB7 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, William Albert4, Albert Roy3, George Washington2, Andrew S.1
1 STRAUB 23492 EJJQA 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     12 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, William Albert4, Albert Roy3, George Washington2, Andrew S.1
STROUP 124348 2KGR5 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 24 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, Charles Henry4, William Hostetler3, Levi B.2, Moses1
STROUPE 118841   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 14 8 13 26 20 14 13 11 12 10 12 12 11 Pvt11, Pvt10, Paul Clifton9, William Henry8, Silas7, Joseph6, Adam5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STRAUB 32866 87BF4 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 21 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt10, Walter Larue9, Lewis8, Samuel Daniel7, Isaac6, Joh. Heinrich5, Joh. Carl4, Joh. Pieter I3, Hans Adam2, Martin1
CRUMP 50052 WD24Q 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 36 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt4, Pvt3, Richard Lexington2, William Waitsel1 PRESTWOOD-CRUMPpresumed descendant of Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STROUPE 74957 RMR7C 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 15 13 11 12 10 12 12 11 Pvt10, Andrew Jackson9, Alfred Isaiah8, Ephraim Daniel7, Matthew Wallace6, Daniel5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STROUP 24212 345AZ 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 25 20 14 13 11 12 10 12 12 11 Pvt10, Lawrence Everett9, David King8, Adam7, Andrew Adam6, Adam5, Joh. Pieter II4, Joh. Pieter I3, Hans Adam2, Martin1
STROUPE 130123 3NQW5 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8 10 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt8, Pvt7, Sidney Crockett6, William Henry5, Charles H.4, Andrew3, John2, John Peter1
STROUP 138214  NNNEK 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8 10 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt12, Pvt11, Clementine T.10, William Aheart9, Sylvester Aheart7, Philip6, Philip5, Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
STROUP 116646   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 20 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt12, Pvt11, Goodell Wilson Jennings10, Clay Goodelle9, Wilson W.8, Samuel7, Peter6, Andrew5, Joh. Pieter II4, Joh. Pieter I3, Hans Adam2, Martin1
STRAUB 111298 47F2N 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 20 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt11, Pvt10, Otto Ludwig9, Johann Ludwig8, Philipp Dietrich7, Philipp Dietrich6, Georg Michael5, Georg Adam4, Antonius3, Hans Adam2, Martin1
2 STROUP 23426 T7TGS 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 28 12 14 15 15     11 10 19 21 14 14 15 20 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt6, Roland Virgil5, Henry Burdett4, Henry3, Samuel2, George1
STRAUB 75122   14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 21 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 16 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, Harold Henry4, Samuel3, John Jr.2, John Sr.1
STROUPE 133507 KSRGY 14 22 15 11 13 13 11 16 11 12 11 28 15 8 9 8 11 22 16 19 29 12 14 15 15 12 15 11 10 19 21 14 14 15 21 35 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 26 20 14 13 11 12 10 12 12 11 Pvt5, Pvt4, Russell B.3, Aaron2, Elisha1presumed descendant of Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
3 BARNES 119218   14 22 15 11 13 13 11 16 11 13 11 29 15 8 9 8 11 22 16 19 29 12 14 15 15     11 10 19 21 14 14 15 21 34 35 12 10 11 8 15 15 8 11 10 8  9 9 12 22 25 15 10 12 12 15 8 13 25 20 14 13 11 12 10 12 12 11 Miles Raymond11, Myles Raymond10 STROUP-BARNES, Robert Daniel9, George W.8, Daniel S.7, Peter6, Adam5, Joh. Peter II4, Joh. Peter I3, Hans Adam2, Martin1
? STROUPE 122322   14 22 15 11 13 13 11 16 11 12 11 28                                                                                                                   Pvt10, Pvt9, Jasper Daniel8, Daniel Jasper7, George6, Jacob5, Joh. Pieter II4, Joh. Pieter I3, Hans Adam2, Martin1
CRUMP 138239   14 22 15 11 13 13 11 16 11 12 11 28                                                                                                                   Pvt3, Richard Lexington2, William Waitsel1 PRESTWOOD-CRUMPpresumed descendant of Joh. Jacob I4, Joh. Pieter I3, Hans Adam2, Martin1
The BARNES has what appears to be a genetic distance of four, but it's actually three because any mutation in DYS389i is reflected in DYS389ii, so the differences in those markers represent one mutation event, not two.
#133507 has two additional copies of DYS464.  This is a rare condition, with only about 1.5% of people tested having more than four copies at this location.  FTDNA scores this difference as a Genetic Distance of two from the modal haplotype, but it's entirely possibly that the two additional copies appeared in one mutation event (by duplication of the 12 allele and one of the 15 alleles).  The testing of cousins could prove whether this condition is the result of one mutation event or two, but it is most likely one.
The three cells highlighted in orange pose a challenge for interpreting the results in view of what are believed to be the relationships between these individuals.  If only #111298, the STRAUB still living in Wuerttemberg and descended from Antonius, brother of Johann Pieter, had this value, there would be no quandry.  We could simply assume his value of 20 at DYS570 stems from a mutation between Antonius and the test subject.  Even the matching value for #23426 is not a serious problem, because we can postulate that Antonius had the ancestral haplotype, and Johann Pieter is the one with the mutation (from 20 to 21), and that George must descend from some other member of this family who immigrated to the U.S., not Johann Pieter.  It's #116645 that poses the problem because he has a paper connection to Johann Pieter, yet possesses a value of 20 at DYS570.  To maintain the existing paper connections, we have to accept that the same mutation happened independently three times in the same family in only a dozen generations, the probability of which is low, even if we take into account that DYS570 is one of the fasted mutating markers.  The issue could be resolved if #23426 and #116645 would max out their markers.  I discuss this problem further on the Node Chart for the Descendants of Martin STRAUB.
Results for descendants of Jacob STROUP I (1722-1804/5) of Lincoln [now Gaston] Co., NC, purported grandson of Matthias STROOP, the 1687 immigrant from Westphalia to Maryland, were unexpected because, as you can see above, they are a tight match (66/67 and 67/67) for the descendants of Johann Pieter STRAUB I of Pennsylvania.  These two are a decided non-match with the descendants of Jacob STROUP II (1771-1846) of NC, who are Haplogroup J2.  Being in different haplogroups means these I1 and J2 individuals cannot have shared a common ancestor for thousands of years, which means Jacob STROUP II cannot be a grandson of Jacob STROUP I as formerly believed.  These results resurrect and support the assertion that Jacob STROUP I of NC is the missing son, Johann Jacob STRAUB, who immigrated to Philadelphia in 1733 with his father, Johann Pieter STRAUB I.
Results for #75122 were also unexpected because he is not a match with the other paper descendant of John STRAUB, Sr., of Beaver Township (see Haplogroup I1-Norse-D, #24343, below). Because #75122 descends through John Jr., whose paper connection to John Sr. is essentially unassailable, it appears (for that and other reasons) that #24343 is the one with the bad connection to John Sr. For more discussion on the matter, please see John Sr.'s family group sheet
#133507 was originally tested at Ancestry-DNA and has now been re-tested at FTDNA.  He is a descendant of Elisha STROUP, whom I have long contended could not be a son of Jacob STROUP II as shown by most sources (all secondary).  My reasoning had been that Jacob II's wife at the time Elisha was born was simply too old to be bearing children.  The DNA test results support this contention because Elisha's descendant is Haplogroup I1 and matches this family, while Jacob STROUP II's descendants are Haplogroup J2.  People in different haplogroups cannot have shared a common ancestor for thousands of years.  I implore everyone considering being tested to do so with FTDNA, from the start; otherwise, you will likely end up having to do what this individual has had to do, that is, having to pay for being tested twice.  If you have any intention of eventually joining this project, it's invariably going to end up being false economy to get tested elsewhere, first.
Another unexpected result is the match with #97358, surnamed BELEW.  The match is 67/67 leaving no doubt that he is closely related to the other individuals in this table.  It does appear this individual has an NPE in his lineage, and it's not insignificant that, for decades, the BELEWs lived in close association with the STROUPs of Jefferson Co., MO
A further unexpected result is the match with #50052, surnamed CRUMP, who apparently has an NPE in his lineage.  Some further testing of cousins is needed to pinpoint the STROUP in his patrilineal line.  His father haas been tested (#138239), and he, too, is a STROUP.
Results for #130123 support the contention of early researchers that the John Peter STROUP of Wythe Co., VA, is a member of this family, though is possibly not connected to it in the way envisioned (see next entry).  Two other paper descendants of John Peter have been tested, and each has an NPE in his lineage (see Node Chart for John Peter).
#138214 shares a mutation with the above #130123 (red table cells).  The problem is, either we again have a situation where we have to postulate that the same mutation happened more than once in a few generatons, or there is something wrong with their paper genealogy.  The latter is far more probable.
Three of the above individuals have been deep SNP tested, namely, #26156, #23492, and #24212; and, as expected, they all had the same results:
P19+ M170+ M258+ P30+ P38+ M253+ M307+ M21- M72- M227- P37.2- M26- M161- M223-
The positive SNP tests prove they are I1 (see I1 table).  The negative results for M21, M72, and M227 rule out their belonging to any known subclade of I1, which means, based on the current haplogroup tree, they are root/ancestral I1*.  The remaining negative results rule out their being any form of I2 (see I2 table). 

With two separate lines now deep SNP tested (one line redundantly, in the case of the two brothers), the probability that the remaining descendants of Johann Pieter will have the same SNP test results is a virtual certainty.  Also, keep in mind that an STR value of 8 at DYS455 makes being Haplogroup I1 a virtual certainty.  Therefore, your project admin recommends that other members of this family invest in testing advanced STR markers, rather than SNP testing

#23492 has been ordering advanced Haplogroup I SNPs as they become available from EthnoAncestry:
S62+ S63+ S64+ S65+ S66+ S107+ S108+ S109+ S110+ S111+ P40+ P109- P259-
So far, the ten S-series SNPs have simply proven to be redundant for determining I1, (see table above).  Our subject is negative (ancestral) for P109 and P259, so he remains root I1*.  Being negative (ancestral) for the last two is, so far, correlated with being one of the AngloSaxon varieties of I1. 
As of Oct 2008, the "Deep-Clade-I" test at FTDNA consists of a different suite of SNPs than those tested above.  The CRUMP (#50052) has undergone these tests:
P30+ M253+ M21- M227- P109- P259-
The positive SNPs prove he is I1; the negative SNPs prove he is no known subclade of I1, confirming he, too, is root/ancestral I1*. 
Because we have four different lines in this family matching 67/67, we need to find more markers to separate them.  With the purchase of DNA-Fingerprint (in July of 2006), Family Tree DNA began offering DNA-FP's extensive suite of "advanced" DNA tests.  Hopefully, some of these markers will give us the separaton we need.  In terms of determining modality of markers, the two brothers should really be considered as one indicator.  So, given that their results are identical, I have lumped the two brothers together in the "advanced" marker tables.
Among the Y-DNA "Advanced Tests" offered by FTDNA are the nine markers tested by SMGF (the Sorensen Molecular Genealogy Foundation) that are not among the Standard 67 markers tested by FTDNA.  SMGF has a huge online database, so when choosing additonal markers to test, the logical first choice would be to test these nine markers, especially as the SMGF database is the one most relied upon by Nordtvedt in defining varieties of Haplogroup I.  So far, three of our members have opted for these nine tests:
The Nine "Missing" SMGF Markers from DNA-FP
Surname Kit # Ysearch
User ID
4
6
1
4
6
2
A10
|
G
A
T
A
C4
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6
3
5
GG
AA
T-
1B
07
4
4
1
4
4
5
4
5
2
4
6
3
I1-AS5 Modal Values 12 12 13 21 11 16 11 31 21
STROUP 78741 H5K5T 12 13 14 21 11 16  9 31 21
STRAUB
brothers
26156
23492
BUHB7
EJJQA
12 13 14 21 11 16  9 31 21
STRAUB 111298 47F2N 12 13 14 21 11 16  9 31 21
STROUP 133507 - 12         16     21
The two brothers match, as expected, but so does #78741 and #111298, so we didn't get the separation we were looking for.  A check at Ysearch and SMGF shows that they have no matches in either database for these nine markers and that it's the value of 9 at DYS445 that's preventing them from having any matches because this value is very rare.  Overall, using the SMGF database figures (as of July 2008), only 16 people out of 21,006 people tested (0.076%) are 9 at this marker.  Within Haplogroup I1, this family is unique in having a value of 9 at this marker.  We also have an unexpected value for DYS462.

There are two markers that strongly separate Nordtvedt's AngloSaxon (AS) varieties from his Norse/ultraNorse (N/uN) varieties.  These are DYS511 and DYS462, which are 9,12 in AS and 10,13 in N/uN (I've color-coded the table cells "kelly green" for AS and "royal blue" for N/uN).  What's interesting is that this STRAUB/STROUP family is typically AngloSaxon for DYS511 (the column of 9's highlighted in kelly green in the main table above), but typically Norse/ultraNorse for DYS462 (the column of 13's highlighted royal blue in the small table here).

EthnoAncestry (EA) tests ten STR markers formerly not tested by any other laboratory; they are now offered by FTDNA among their Advanced tests as "Y-STR DNA-FP Panel 9." 
EthnoAncestry "YSTR FT Upgrade"  =  FTDNA "Panel 9"
(Markers in red are fast mutating. Modals per Nordtvedt, 4 Aug 2007.)
Surname FTDNA # Ysearch
User ID
4
9
4
5
0
5
5
2
2
5
3
3
5
4
9
5
5
6
5
7
5
5
8
9
6
3
6
6
3
8
I1 modal values 9 11 11 11 13 12 10 13 11 12
STROUP 78741 H5K5T 9 11 11 11 13 12 10 13 11 12
STRAUB
brothers
26156
23492
BUHB7
EJJQA
9 11 11 11 13 12 10 13 11 12
STRAUB 111298 4752N 9 11 11 11 14 12 10 13 11 12
 
Legend for Colors:
Pale Blue Pale blue is the background color for this family in this table, in the Census Tables, and elsewhere on this web site.
It is also the background color for the values of the modal haplotype for AngloSaxon-5.
Light Purple Characteristic marker values distinguishing this family from modal AngloSaxon-5.
Kelly Green Characteristic marker values distinguishing Anglo-Saxon from Norse and ultraNorse.
Royal Blue Characteristic marker values distinguishing Norse and ultraNorse from AngloSaxon.
Bright Blue A mutation distinguishing this person from others in the family, a.k.a., a "private" mutations.
Bright Yellow A mutation distinguishing descendants of Adam5, Joh. Pieter II4, Joh. Pieter I3, Hans Adam2, Martin1
Deep Pink A mutation distinguishing the Wuerttemberg STRAUB from the American STRAUBs.
Orange A mutation that remains unexplained because it is not congruent with the paper genealogy.
 
In an attempt to find a mutation separating them, these three members have opted to take ten more Y-STR tests from the DNA-FP "Advanced" marker panels at FTDNA.  Modal values in the table below are calculated from the Ymatch database at DNA-FingerPrint (as of 14 Dec 2007).
Ten Y-STR DNA-FP Markers from FTDNA
Surname Kit # Ysearch
User ID
DXYS
156-Y
4
3
4
4
3
5
4
8
5
4
9
5
6
4
3
7
1
4
7
1
6
7
1
7
7
2
6
I1 Sample Size per Marker 6 10 8 11 11 15 11 10 10 13
I1 Modal Values 12  9 11 12 17 12 24 27 19 12
STROUP 78741 H5K5T 12  9 11 12 18 12 24 27 19 12
STRAUB
brothers
26156
23492
BUHB7
EJJQA
12  9 11 12 18 12 24 27 19 12
STRAUB 111298 4752N 12  9 11 12 18 12 24 27 19 12
 
The Y-STR DNA-FP Panel 5 Palindromic Pack from FTDNA returns values for 33 markers (lower case letters designate specific nucleotides).  Nine of these tests are redundant from other panels (the table cells shaded in grey), so the total number of "new" markers is actually 24.  We do, at last, have separation!
Palindromic Pack from FTDNA
Surname Kit # Ysearch DYF
371X
DYF
385
DYF
397
DYF
399X
DYF
401
DYF
408
DYF
411
DYS
413
DYS
464X
DYS
724
DYS
725
I1 Modals compiled from Ymatch* 10c 12t 13c 14c 10 10 12 13 14 14 22t 24c 25c 16 17 188 188  9 13 13 13 23 25 - - - - 35 37 30 32 32 32
STROUP 78741 H5K5T 10c 12t 13c 14c  9 10 12 13 14 15 22t 26c 26c 16 17 188 188 11 14 13 13 22 25 12g 14g 15g 15g 35 35 29 30 32 32
STRAUB
brothers
26156
23492
BUHB7
EJJQA
10c 12t 13c 14c  9 10 12 13 14 14 22t 24c 25c 16 17 188 188 10 13 13 13 22 25 12g 14g 15g 15g 35 35 29 30 32 32
STRAUB 111298 4752N 10c 12t 13c 14c  9 10 12 13 14 15 22t 26c 25c 16 17 188 188 10 13 13 13 22 25 12g 14g 15g 15g 35 35 29 31 32 32
The redundant markers are:  the 12t value for DYF371X, which is the DYS425 value from Markers 38-67, plus the nucleotide designation; DYS413, which is duplicated from Markers 38-67; DYS464X, which is duplicated from Markers 13-25, but with the addition of the nucleotide designations, so it's not really a redundant test; DYS724, which is duplicated from Markers 26-37 where it is designated CDYab.

In the case of DYF399X, the actual order of the three alleles is not known.  By convention, they are reported in alphanumeric order.  I have ordered them to have the least possible differences between them, beginning with the modal haplotype as the base.



*The number of individuals who have tested these markers is low, so the modals I've compiled are not statistically valid, but they're all I've got.  They are least meaningful for DYF399X, so they would be worth recalculating at some point for this marker especially.


What constitutes a match?
Matches in other surnames are usually mere coincidence, so please ignore them — I'll let you know when you shouldn't!
For 12 markers:  9 or less is a non-relative; 10-12, please see this Chart compiled by FTDNA.
For 25 markers:  21 or less is a non-relative; 22-25, please see this Chart compiled by FTDNA.
For 37 markers:  31 or less is a non-relative; 32-37, please see this Chart compiled by FTDNA.
For 67 markers:  55 or less is a non-relative; 56-67, please see this Chart compiled by FTDNA.
For any test:  0 matching markers, please contact NASA.

 
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