Variant DetailsVariant: esv3622103Internal ID | 6662273 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 434 | hg19 | 434 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13665670, essv13665666, essv13665671, essv13665676, essv13665674, essv13665677, essv13665661, essv13665662, essv13665667, essv13665673, essv13665669, essv13665663, essv13665665, essv13665668, essv13665678, essv13665672, essv13665664, essv13665675 | Samples | HG02035, NA18641, HG01944, NA20850, HG02131, HG01813, HG02187, HG00530, HG02136, HG02142, HG01857, HG02397, HG02165, HG01596, HG01597, HG01872, HG02028, NA18549 | Known Genes | ADARB2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622103
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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