Variant DetailsVariant: esv3643668 Internal ID | 6683739 | Landmark | | Location Information | | Cytoband | 19p13.2 | Allele length | Assembly | Allele length | hg38 | 1861 | hg19 | 1861 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15990779, essv15990717, essv15990758, essv15990760, essv15990748, essv15990757, essv15990750, essv15990741, essv15990732, essv15990755, essv15990733, essv15990768, essv15990736, essv15990762, essv15990764, essv15990718, essv15990754, essv15990782, essv15990719, essv15990743, essv15990712, essv15990723, essv15990715, essv15990746, essv15990720, essv15990734, essv15990766, essv15990774, essv15990753, essv15990735, essv15990780, essv15990744, essv15990731, essv15990778, essv15990739, essv15990740, essv15990725, essv15990751, essv15990749, essv15990773, essv15990713, essv15990772, essv15990770, essv15990745, essv15990747, essv15990714, essv15990776, essv15990742, essv15990771, essv15990761, essv15990711, essv15990765, essv15990781, essv15990763, essv15990737, essv15990756, essv15990767, essv15990724, essv15990738, essv15990777, essv15990775, essv15990722, essv15990727, essv15990726, essv15990728, essv15990752, essv15990769, essv15990759, essv15990721, essv15990716, essv15990729, essv15990730 | Samples | NA19394, NA18502, NA19399, HG03449, NA18917, NA20298, NA19393, HG03100, NA18870, HG03199, NA19446, HG03168, HG02952, HG02595, NA18916, HG02054, NA18498, HG03520, NA18868, HG02885, NA19207, NA19172, HG01176, NA19189, HG02545, NA19025, HG03114, HG02819, HG02442, NA19707, HG03061, NA19184, HG02449, HG01882, NA19455, HG02450, NA18871, HG02497, HG03124, HG02555, HG03202, HG02577, HG03388, NA19113, NA18853, HG03046, NA19452, HG03109, HG01204, NA19035, NA19308, HG02557, HG03367, NA19454, NA18865, NA19835, HG01342, HG03103, NA19475, NA19818, NA19376, NA19328, HG03112, NA20334, HG02013, NA19030, NA19146, HG01886, HG03198, HG02808, HG03439, HG03196 | Known Genes | TSPAN16 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3643668
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 72 | Observed Complex | 0 | Frequency | n/a |
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