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Lineages and Results of Y-chromosome DNA Testing for Surname CARRIÇO
Haplogroup I1
Results
Hub
Y-DNA Haplogroups Represented in the Project
(sample size = number tested inside the project + number tested outside the project)
Project
Home
I1d
(n=1)
J2a4
(n=1)
J2a4b
(n=24+1)
J2a4b1
(n=1)
L2a
(n=2)
R1b1*
(n=1+1)
R1b1a2
(n=6)
Haplogroup I is found almost exclusively in Europe where it is represented in about 20% of the population.  Its strong geographic concentration in northwestern Europe has led Hg I to be nicknamed the "Viking" haplogroup (though some consider R1a to be the only true Viking haplogroup).

I1 is the most common subclade of Hg I.  Geographically, it is highly concentrated in northern Germany, Denmark, and southern Norway and Sweden.  Most individuals who are Haplogroup I1 will be I1*, that is, root/ancestral I1.  Only a few SNPs usefully divide Hg I1, namely L22 and P109, which appear most freqently in Scandinavia and define I1d and I1d1, repectively (see SNP table below).

Among European haplotypes, DYS455=8 is virtually exclusive to I1 and YCAIIa,b=19,21 is universal in I1 (table cells highlighted in red).  In lieu of useful SNPs (the search for which is ongoing), varieties of I1 have been defined by Nordtvedt based on STR haplotypes.  Another useful marker in this subclade is DYS511 (highlighted in royal blue in the tables), which has a value of 10 in the Norse and ultraNorse varieties and a value of 9 in the AngloSaxon varieties — 11 is rare. DYS462 is similarly useful in separating AngloSaxon and Norse varieties and can be ordered as an "Advanced" test from FTDNA.

We have one member of the CARRICO project who is Haplogroup I1, and deep SNP testing shows him to be L22+, that is, I1d.  Cullen's predictor gives him the highest probability of being I1d-NuN14.  The Norse and ultra-Norse varieties of I1d are most common in Norway.

Some researchers believe Hg I1 took refuge on the Iberian Peninsula during the LGM (Last Glacial Maximum) ca. 18,000 yrs ago.  Others believe the emergence of I1 came much later.  The current distribution if I1 show it only barely represented in Iberia (see map for European distribution of Hg I1).

I would recommend anyone interested in Haplogroup I subscribe to the Y-DNA-HAPLOGROUP-I mailing list at RootsWeb to learn more about this subclade (Ken Nordtvedt is a subscriber there).
Y-DNA Haplogroup I1 SNPs and Subclades
Mutations Haplogroup
ISOGG FTDNA
M170=PF3715 P19_1-5 L41=PF3787 M258 P212 P38 PS76 U179 I I
____ M253 L64 L75 L80 L81 L118 L121=S62 L123 L124=S64 L125=S65 L157.1 L186 L187 L840
M307.2=P203.2 M450=S109 P30 P40 S63 S66 S107 S108 S110 S111
I1 I1
____ DF29=S438 I1-a  
____ Z2336=CTS6364 I1-a1  
____ M227 I1-a1a I1b 
____ M72 I1-a1a1 I1b1
L22=S142 I1-a1b I1d
____ P109 I1-a1b1 I1d1
L205 I1-a1b2 I1d2
L287 I1-a1b3 I1d3
____ L258=S335 I1-a1b3-a I1d3a
____ L296 I1-a1b3-a1  
L300=S241 I1-a1b4 I1d4
L813=Z719 I1-a1b5  
L211 [private] - I1e
Z58=S244 I1-a2   
____ Z59=S246 I1-a2a  
____ Z60=S337 Z61=S439 Z62 I1-a2a1  
____ Z140 Z141 I1-a2a1-a  
____ Z2535 I1-a2a1-a1  
____ L338 I1-a2a1-a1a  
Z2538=CTS10937 I1-a2a1-a1b  
F2642 I1-a2a1-a2  
____ L592 [private: STRAUB family]     
Z73 I1-a2a1-b  
L573 I1-a2a1-c  
L1248 I1-a2a1-d  
____ L803 I1-a2a1-d1  
Z382 I1-a2a2  
S296=Z138 Z139 I1-a2b  
____ Z2541 I1-a2b1  
Z63=S243 I1-a3  
____ L1237 I1-a3a  
Z131 I1-b  
P215 I2 I2
To view more of the page without scrolling, temporarily reduce the text size or page size in your browser.  Red labels indicate markers that typically mutate more frequently than those labeled in black.  (Empty cells that are darkened indicate tests not ordered.)  Keywords for search engines: genetic genealogy.

Haplogroup I1d  =  I-L22
I1d-Norse/ultraNorse-14 Cluster
To view lineages, please scroll to the right.
Surname Kit # Ysearch
Code
Haplotype — as determined by STR testing Known Lineage
Panel 1:  Markers 1-12 Panel 2:  Markers 13-25 Panel 3:  Markers 26-37 Panel 4: Markers 38-67
3
9
3
3
9
0
19
/
3
9
4
3
9
1
a
|
3
8
5
b
|
3
8
5
4
2
6
3
8
8
4
3
9
i
|
3
8
9
3
9
2
ii
|
3
8
9
4
5
8
a
|
4
5
9
b
|
4
5
9
4
5
5
4
5
4
4
4
7
4
3
7
4
4
8
4
4
9
a
|
4
6
4
b
|
4
6
4
c
|
4
6
4
d
|
4
6
4
4
6
0
H4
|
G
A
T
A
IIa
|
Y
C
A
IIb
|
Y
C
A
4
5
6
6
0
7
5
7
6
5
7
0
a
|
C
D
Y
b
|
C
D
Y
4
4
2
4
3
8
5
3
1
5
7
8
a
|
S1
3
9
5
b
|
S1
3
9
5
5
9
0
5
3
7
6
4
1
4
7
2
S1
4
0
6
5
1
1
4
2
5
a
|
4
1
3
b
|
4
1
3
5
5
7
5
9
4
4
3
6
4
9
0
5
3
4
4
5
0
4
4
4
4
8
1
5
2
0
4
4
6
6
1
7
5
6
8
4
8
7
5
7
2
6
4
0
4
9
2
5
6
5
Modal I1d-NuN14 Haplotype 13 23 14 10 14 15 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 14 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 17 8 12 26 20 13 14 11 12 11 11 12 11 as per Nordtvedt
               
CARRIÇO 176551 A96ST 13 24 14 10 14 14 11 14 12 13 11 30 16 8 9 8 12 23 16 21 29 12 14 14 16 10  9 19 21 14 14 17 20 33 38 12 10 11 8 15 15 8 11 10 8  9 11 12 23 25 15 10 12 12 16 8 12 25 20 13 14 11 12 11 11 12 11 Pvt… CARRIÇO — of Portel, Alentejo, Portugal
Using Jim Cullen's Haplo-I Cluster Predictor, he most resembles:  I-L22-NuN-14 =>36%,
which is consistent with his value of 14 at DYS617 (yellow table cells).
Our subject has no remotely significant matches in the FTDNA, Ysearch, or SMGF databases (as of 17 Dec 2010).
Any change in DYS389i is reflected in DYS389ii, so a change from 12/29 to 13/30 is actually one mutation event (in DYS389i), not two.
Deep SNP testing shows him to be L22+ and P109-.
   

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; for 10-12 markers, please see this table compiled by FTDNA.
For 25 markers: 21 or less is a non-relative; for 22-25 markers,
For 37 markers: 31 or less is a non-relative; for 32-37 markers,
For 67 markers: 59 or less is a non-relative; for 60-67 markers,
For 111 markers: 100 or less is a non-relative; for 101-111 markers,
For any test:  0 matching markers, please contact NASA.

 

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