Variant DetailsVariant: esv3615837Internal ID | 6656035 | Landmark | | Location Information | | Cytoband | 8p23.3 | Allele length | Assembly | Allele length | hg38 | 970 | hg19 | 970 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13061680, essv13061681, essv13061687, essv13061686, essv13061689, essv13061683, essv13061691, essv13061685, essv13061690, essv13061684, essv13061679, essv13061688, essv13061682 | Samples | NA19819, HG03224, HG02108, HG03397, HG01286, NA19318, HG02255, HG03028, NA19376, NA19900, HG01125, NA19346, NA19431 | Known Genes | DLGAP2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3615837
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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