What relevance is a big Y test with 12 shared novel variations and 1 variation that is not shared with any?
Big Y SNP question
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The non-matching SNP can be ignored. The algorithm that looks for matching and mismatched SNPs has bugs. You need an expert to look at your VCF or BAM files. Have you contacted your haplogroup admin or have you sent your BAM file to www.yfull.com ? Are you in a subclade of P312?
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Originally posted by Armando View PostThe non-matching SNP can be ignored. The algorithm that looks for matching and mismatched SNPs has bugs. You need an expert to look at your VCF or BAM files. Have you contacted your haplogroup admin or have you sent your BAM file to www.yfull.com ? Are you in a subclade of P312?
Thanks for the reply, will check into the P312
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Originally posted by Wheal View PostYes I have had my (Dad's) BAM file sent to yfull but I am not in a subclade of P312, and someone has looked at the BAM file, no comments from them. It was a very confusing origins report... no German at all... and we know the family there... must be an NPE from Sweden...
Thanks for the reply, will check into the P312
Have you contacted your matches to see if they have also sent their BAM files to YFull? That would allow YFull to name shared SNPs that haven't been named and provide a TMRCA with your matches.
Do you mean myOrigins when you refer to a very confusing origins report? Autosomal DNA calculators have a very hard time identifying German DNA no matter which company is used. Also if the German ancestry is several generations back then it can get diluted due to non-German ancestry.
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