Variant DetailsVariant: esv3640681Internal ID | 6680767 | Landmark | | Location Information | | Cytoband | 17q21.31 | Allele length | Assembly | Allele length | hg38 | 31805 | hg19 | 31805 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv576e214 | Supporting Variants | essv15684479, essv15684470, essv15684471, essv15684487, essv15684484, essv15684474, essv15684477, essv15684486, essv15684468, essv15684481, essv15684478, essv15684482, essv15684469, essv15684480, essv15684488, essv15684475, essv15684472, essv15684476, essv15684483, essv15684485, essv15684473 | Samples | HG01465, NA21137, NA20863, HG03645, NA12812, HG04022, HG03874, NA21108, HG02490, HG03888, HG02780, NA20854, NA20787, NA20524, HG03760, HG02789, HG00740, NA20534, NA20765, HG03949, HG01113 | Known Genes | KANSL1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3640681
| Frequency | Sample Size | 2504 | Observed Gain | 21 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|