Variant DetailsVariant: esv3638110 Internal ID | 6678208 | Landmark | | Location Information | | Cytoband | 16p12.3 | Allele length | Assembly | Allele length | hg38 | 45849 | hg19 | 45849 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15397763, essv15397731, essv15397796, essv15397746, essv15397747, essv15397805, essv15397786, essv15397754, essv15397795, essv15397764, essv15397810, essv15397750, essv15397766, essv15397804, essv15397770, essv15397812, essv15397756, essv15397749, essv15397758, essv15397735, essv15397783, essv15397814, essv15397788, essv15397752, essv15397728, essv15397813, essv15397774, essv15397785, essv15397780, essv15397765, essv15397762, essv15397743, essv15397799, essv15397737, essv15397759, essv15397802, essv15397791, essv15397771, essv15397755, essv15397740, essv15397772, essv15397781, essv15397807, essv15397782, essv15397767, essv15397734, essv15397798, essv15397741, essv15397736, essv15397732, essv15397779, essv15397730, essv15397794, essv15397738, essv15397792, essv15397773, essv15397790, essv15397769, essv15397753, essv15397803, essv15397761, essv15397800, essv15397801, essv15397775, essv15397768, essv15397789, essv15397777, essv15397811, essv15397751, essv15397797, essv15397733, essv15397739, essv15397808, essv15397742, essv15397748, essv15397757, essv15397760, essv15397778, essv15397784, essv15397809, essv15397776, essv15397745, essv15397744, essv15397806, essv15397793, essv15397729, essv15397787 | Samples | HG00881, HG00442, HG03121, HG02072, HG01860, HG02122, HG02029, NA18979, NA18641, NA18603, HG01806, NA18633, HG03944, HG02023, HG00717, HG00622, NA19792, HG00589, HG02185, HG02140, HG00599, HG03485, HG02549, HG01840, NA19681, HG03762, HG00590, HG03520, HG02395, HG02389, HG02187, HG00534, NA18617, NA19317, HG03777, HG02471, HG03814, HG02502, HG03832, NA18638, HG02134, HG02166, HG02570, HG00629, NA19056, HG00701, HG01810, HG00584, HG00533, HG00500, NA20126, NA18976, NA20770, HG00708, HG01102, NA21124, HG01241, NA19320, HG02081, NA19318, NA19395, NA18570, NA18974, NA20296, HG00476, HG03833, NA18952, HG01878, NA18950, HG01362, NA19439, NA19786, HG02137, HG02019, NA19376, NA19328, NA19078, HG03565, HG03066, NA20849, NA18987, HG02392, HG03925, HG03077, HG00759, HG01805, NA18562 | Known Genes | ABCC6P1, NOMO2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638110
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 87 | Observed Complex | 0 | Frequency | n/a |
|
|