Добрый день! Готов тест сынишки. FTDNA 67 маркеров. Определили I2a (P37.2+)

:
Очень хочется опредеить субклад точнее. Возможно ли это сделать по этим данным

. Или надо заказывать снипы. Подскажите плиз.

1 2 3 4 5 6 7 8 9 10 11 12
DYS# 393 390 19* 391 385a 385b 426 388 439 389-1 392 389-2
Alleles 13 24 15 11 14 15 11 13 13 13 11 30
PANEL 2 (13-25)
Locus 13 14 15 16 17 18 19 20 21 22 23 24 25
DYS# 458 459a 459b 455 454 447 437 448 449 464a** 464b** 464c** 464d**
Alleles 17 8 10 11 11 25 15 21 31 12 14 15 16
PANEL 3 (26-37)
Locus 26 27 28 29 30 31 32 33 34 35 36 37
DYS# 460 GATA H4 YCA II a YCA II b 456 607 576 570 CDY a CDY b 442 438
Alleles 10 10 21 21 16 12 18 18 32 35 11 10
PANEL 4 (38 - 47)
Locus 38 39 40 41 42 43 44 45 46 47
DYS# 531 578 395S1a 395S1b 590 537 641 472 406S1 511
Alleles 11 8 15 15 7 12 10 8 12 9
PANEL 4 (48 - 60)
Locus 48 49 50 51 52 53 54 55 56 57 58 59 60
DYS# 425 413a 413b 557 594 436 490 534 450 444 481 520 446
Alleles 12 21 22 16 10 12 12 13 7 10 29 21 13
PANEL 4 (61 - 67)
Locus 61 62 63 64 65 66 67
DYS# 617 568 487 572 640 492 565
Alleles 14 10 13 11 11 12 9
*Also known as DYS 394
**On 5/19/2003, these values were adjusted down by 1 point because of a change in Lab nomenclature.
***A value of “0” for any marker indicates that the lab reported a null value or no result for this marker. All cases of this nature are retested multiple times by the lab to confirm their accuracy. Mutations causing null values are infrequent, but are passed on to offspring just like other mutations, so related male lineages such as a father and son would likely share any null values