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Lineages and Results of Y-chromosome DNA Testing for Surname CARRICO
and Similar Surnames, such as, CARRIÇO, CARRICOE, CURRICOE, CARICO, CARUCHO, CARACO, CARAÇO, CARRACO, CARACHO, KARAHO, CARASSO, CARAÇOS, CARICCO, etc.
Haplogroup L
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Y-DNA Haplogroups Represented in the Project Project
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 J2  (n = 7)  L  (n = 2)
Haplogroup L descends from Haplogroup K and is believed to have first appeared about 30,000 years ago.  Because it is most common in southern and western Indian, Haplogroup L is sometimes called the "Indian Clan," alhough it is also found across central and southwestern Asia and thinly across southern Europe.  Marco Cagetti has an informative web site on Haplogroup L; and, of course, there is the Haplogroup L DNA Project run by Gareth Henson.  Haplogroup L is divided into three main subclades:  L1, L2, and L3.

L1 is the common subclade in India, while L3 has its highest concentration in Pakistan.  L2 is the predominant subclade for European Haplogroup L, although it is rare at only 1-3% of the population.  L2a is a subclade sometimes called "Mediterranean" because it occurs in southern Europe, from Portugal to Turkey, in the countries bordering the northern coast of the Mediterranean Sea.  Our two subjects, who have an origin in Turkey, have been SNP tested proving they are Haplogroup L2, and based on their haplotype, they have been deduced to be Haplogroup L2a.

Haplogroup L Subclades as Defined by SNP Mutations
The SNP chart below is based on the ISOGG (International Society of Genetic Genealogy) Haplogroup L SNP chart.  FTDNA does not currently do deep SNP testing for haplogroup L, but the key tests (shown in boldface in the table) can be purchased at EthnoAncestry.
Mutations Clades Main Region
M20, M11, M22, M61, M185, M295 L  
- M76, M27 L1 India, Sri Lanka
M317 L2 southern Europe, Anatolia
- M349 L2a Mediterranean: Portugal to Turkey 
M274 L2b  
M357 L3 Pakistani: Burusho and Pashtuns
- PK3 L3a Pakistani: Kalash
Please note that in the most recent release of the ISOGG haplotree (4 May 2008),
subclades L2a and L2b switched places.
(As we do not yet know which mutation occurred first, M349 or M274, the order of their placement in the hierarchy is entirely arbitrary.)

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Red labels indicate markers that typically mutate more frequently than those labeled in black. Marker 464 mutates most rapidly of all and sometimes has five to seven counts (a-g), not just four (a-d).
(Empty cells that are darkened indicate tests not ordered.)

Haplogroup L2a
Surname Kit # Ysearch
UserID

SNP
Test
Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 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
Haplogroup L2a modals     12 23 14 10 16 18 11 12 11 14 13 30 16 9 9 11 12 25 16 19 30 15 15 17 18 10 10 19 21 15 14 18 14 31 33 11 10 11 8 15 15 7 11 9 8 12 9 13 20 20 14 11 12 12 14 8 11 24 23 13 11 11 14 10 11 12 11 Compiled by DGM from Hap-L project (n=17 at 12; n=9 at 37; n=7 at 67) as of 1 Jun 2008
Anatolian L2 individual PSU3S   12 23 14 10       12 13 14 14 30                                                                                                               Haplotype #318 (Cinnioglu 2003:141), subject of eastern Turkey
                 
CARACO 94500 ZVXAK   12 23 14 10 16 18 11 12 12 14 14 30 18 9 9 11 12 25 16 19 29 14 15 16 17 10 10 19 21 14 14 19 17 33 35 11 10                                                             Pvt4, Pvt3, Eliezer2, Albert1 — of Bursa, Turkey [subject lives in the U.S.]
CARACO 119235 F3NKY M20+ 12 23 14 10 16 18 11 12 12 13 14 29 19 9 9 11 12 25 16 19 29 14 15 16 17 10 10 19 21 14 14 18 17 33 35 11 10                                                             Pvt5, Pvt4, Samuel3, Moïse2, Joseph1 — of Bursa, Turkey [subject lives in France]
These individuals have a rare haplotype with no matches in the FTDNA or Ysearch databases closer than 10/12.  They have only a 6/9 or 8/9 match with the single L2 individual from Cinnioglu's 2003 paper on Anatolian haplogroups (see References at right) — this individual is UserID PSU3S in the Ysearch database.  Based on their haplotype, their haplogroup is deduced to be L2a (thank you, Gareth Henson, for the determination).
#94500 is a practicing Sephardic Jew, and he is one of only two Haplogroup L individuals to join the Sephardic Anusim DNA Project (as of 5/08).  Hirschman & Panther-Yates (see link under References, to the right) mention not one L2 in their paper on Sephardic haplogroups.
#119235 has received a gratis backbone SNP test from FTDNA.  The result of M20+ confirms that he is Haplogroup L.
References:

Cengiz Cinnioglu, et al.  2003.  "Excavating Y-chromosome Haplotype Strata in Anatolia."  Human Genetics 114: 127-148 (online at the web site of the Human Population Genetics Laboratory, Stanford University; n.b., the value for DYS389ii was converted to FTDNA standards using the Ysearch conversion chart).

Elizabeth Caldwell Hirschman & Donald Panther-Yates. Toward a Sephardic Haplogroup Profile in the New World.  (unpublished Word doc online at DNA-Consultants)

 

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:  8 or less is a non-relative; 9-10 means only a small chance of a relationship; 11-12 means a possible relationship.
For 25 markers:  20 or less is a non-relative; 21-22 means only a small chance of a relationship; 23-25 means a possible relationship.
For 37 markers:  30 or less is a non-relative; 31-37, please see this Chart compiled by FTDNA.
For 67 markers:  55 or less is a non-relative; 58-67, please see this Chart compiled by FTDNA.
For any test:  0 matching markers, please contact NASA.

 
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