Из письма Зденко Марковича:
You received your Big Y-700 test result. Your officially confirmed haplogroup is I-Y3118. You do not belong to any known haplogroup below I-Y3118. There are six other I-Y3118 members: Mazalov N116894, Pererva N18656, Latosky 133914, Keller MK14311, Chebotar 219601, Degtariov MI16501 and Tscherkoff who is not a member of our project.
Thanks to your and Latosky's result a new haplogroup below I-Y3118 is identified. You and Latosky share two SNPs. All other I-P37 haplogroup members have negative results for these two SNPs in their Big Y test results.
You and Latosky are in the I-Y39363 haplogroup which is a new haplogroup below I-Y3118. Eventualy, FTDNA will update its haplotree and your new haplogroup will be displayed. Maybe they pick other shared SNP (Y39536) to name your haplogroup. Your haplogroup will be displayed also in the I-P37 haplogroup research blog:
http://i2aproject.blogspot.comThere is another interesting SNP which I found in your VCF file. It is BY35217. This SNP is inside a palindrome region. Palindrome regions are considered as unreliable and SNPs in these regions are not used in phylogeny. You share BY35217+ result with Latosky as well as Pererva and Keller. You have 60 reads at BY35217, 54 reads are positive G+ and 6 are negative A- . Latosky, Pererva and Keller have similar consistency of BY35217 results. Although BY35217 will not be displayed in official haplotrees I think that BY35217 is worth to mention. It shows that Keller and Pereva are your closer match than Chebotar, Mazalov and Degtariov.
You have 11 private variants. One of them is named, it is found also in other unrelated haplogroup.
not sampled in Big Y-500 tests
3809728
C
G
not sampled in Big Y-500 tests
3914418
A
G
not sampled in Big Y-500 tests
4173054
T
C
not sampled in Big Y-500 tests
5180854
G
A
not sampled in Big Y-500 tests
10082093
C
T
11040005
C
T
A5754
13447890
T
C
15598020
G
T
17181435
A
G
not sampled in Big Y-500 tests
19889358
T
G
Latosky has Big Y-500 test result. Six of your private variants are not sampled in that test. Maybe you share some other SNPs which are not covered in Latosky's test.
One of your variants is inside the centromere region (blue). The SNPs in that region are not reliable for phylogeny in some cases.
You can order your BAM raw data file and send it to YFull.com for their interpretation. If you do that you can join YFull's I-L621 group. YFull will compare your result with other results, report the status of unreported SNPs and find novel variants which are not reported because of small number of reads.