Maria,
As per article cited, the D9 STR is located on Chr 9 within a block also defined by SNP's. As 23andMe sequences SNP's and paints the chromosomes the SNP block that includes D9 ought to exhibit the same ancestry as the STR evidences. A 9-repeat STR at D9 is NA and any other repeat within the SNP block on Chr 9 is NA if the SNP block is NA.
Although DeCodeMe does not paint the chromosomes, with some effort one can identify the area of Chr 9 that contains the STR and compare DeCode SNP's to HGDP-CEPH database for indications of ancestry at that SNP block on Chr 9.
Neither of the scanners offer NA as an ancestry definition, East Asian is the closest analog, but HGDP-CEPH does have a couple NA populations.
Announcement
Collapse
No announcement yet.
6 new autosomal STR's from FTDNA
Collapse
X
-
Why not on DeCodeMe?
Tom,
What do you mean by the corresponding snp block of their chromosome 9 and also what do you mean by out of the ordinary repeats? What are the ordinary? I received 6% Asian with DeCodeMe on the autosomal and 9% Asian with the X... Why are those results not accepted...But on 23andme 1% Asian would be...
Maria
Leave a comment:
-
It follows from the above that those without a D9 9 repeat ought not to expect the corresponding SNP block of their Chr 9 will be 'painted' East Asian by 23andMe. But if the other out-of-the-ordinary repeats on D9 have their SNP block painted East Asian this will confirm that those repeats are also potentially Native American.
Leave a comment:
-
This is a For Sale article. if anyone buys it please report back.
Mol Biol Evol. 2009 Feb 17. [Epub ahead of print]
Haplotypic background of a private allele at high frequency in the Americas.
Schroeder KB, Jakobsson M, Crawford MH, Schurr TG, Boca SM, Conrad DF, Tito
RY, Osipova LP, Tarskaia LA, Zhadanov SI, Wall JD, Pritchard JK, Malhi RS,
Smith DG, Rosenberg NA.
Department of Anthropology, University of California, Davis, Davis,
California, United States of America.
Recently, the observation of a high-frequency private allele, the 9-repeat
allele at microsatellite D9S1120, in all sampled Native American and Western
Beringian populations has been interpreted as evidence that all modern Native
Americans descend primarily from a single founding population. However, this
inference assumed that all copies of the 9-repeat allele were identical by descent
and that the geographic distribution of this allele had not been influenced
by natural selection. To investigate whether these assumptions are satisfied,
we genotyped 34 SNPs across approximately 500 kilobases (kb) around D9S1120 in
21 Native American and Western Beringian populations and 54 other worldwide
populations. All chromosomes with the 9-repeat allele share the same haplotypic
background in the vicinity of D9S1120, suggesting that all sampled copies of
the 9-repeat allele are identical by descent. Ninety-one percent of these
chromosomes share the same 76.26 kb haplotype, which we call the "American Modal
Haplotype" (AMH). Three observations lead us to conclude that the high
frequency and widespread distribution of the 9-repeat allele are unlikely to be the
result of positive selection: 1) aside from its association with the 9-repeat
allele, the AMH does not have a high frequency in the Americas, 2) the AMH is
not unusually long for its frequency compared to other haplotypes in the
Americas, and 3) in Latin American mestizo populations, the proportion of Native
American ancestry at D9S1120 is not unusual compared to that observed at other
genomewide microsatellites. Using a new method for estimating the time to the
most recent common ancestor (MRCA) of all sampled copies of an allele on the
basis of an estimate of the length of the genealogy descended from the MRCA, we
calculate the mean time to the MRCA of the 9-repeat allele to be between 7,325
and 39,900 years, depending on the demographic model used. The results support
the hypothesis that all modern Native Americans and Western Beringians trace a
large portion of their ancestry to a single founding population which may
have been isolated from other Asian populations prior to expanding into the
Americas.
PMID: 19221006 [PubMed - as supplied by publisher]
Leave a comment:
-
Originally posted by tomcat View PostBoth your parents had a 16, a repeat count quite common among Europeans and others.
Leave a comment:
-
Originally posted by tomcat View PostMine just came in as 16,16, so both parents were 16,17. And that is ODD as they had ancestries as different as one could imagine.
I ordered mine (batch 291) and my result is the same as yours, 16-16.
I was hoping for a 9.
What does 16 indicate?
Leave a comment:
-
My Autosomal panel 3 results
CD4 6-10
D9S919 18-18
D12S391 15-19
D22S1045 15-17
D10S1248 14-16
D14S1434 13-13
Leave a comment:
-
Originally posted by fmoakesMy wife and I received our AS-3 results.
I am Y-I1*, mt FGS-K1a1, she is mt FGS-T2.
Marker mine hers
CD4 5-6 5-5
D12S391 20-23 18-18
D9S919 14-16 16-17
D10S1248 14-15 13-14
D14S1434 10-13 13-14
D22S1045 15-16 11-16
My AS-panel 3 results:
CD4...............5-6
D12S391.......17-24
D9S919.........16-17
D10S1248......13-14
D14S1434......12-13
D22S1045......15-16
Nas.
Leave a comment:
-
Originally posted by tomcatWith 5 of 7 sibs tested and 4 of those reporting, we have 3 with 16,17 and one with 17,17. ...
Leave a comment:
-
Thank you...
Tom.
Thanks for the update! Sorry to hear you have to retake, waiting for results are frustrating...Hope you get them soon... Goes to show that some fall into the 69% group...
Maria
Leave a comment:
-
Originally posted by Maria_WSo Tom, have you recieved your results back yet? Would you mind posting them all. Did you get a 9 on D9s919? ...
Leave a comment:
-
Results yet?
So Tom, have you recieved your results back yet? Would you mind posting them all. Did you get a 9 on D9s919?
Maria
Leave a comment:
-
The other 69%?
Just curious what other marker combinations the other 69% of Amerindians get?
Maria
Leave a comment:
-
Marker results...
Thank you very much for sharing, appreciate it....
Maria
Leave a comment:
Leave a comment: