Variant DetailsVariant: esv3623834Internal ID | 6664001 | Landmark | | Location Information | | Cytoband | 10q22.2 | Allele length | Assembly | Allele length | hg38 | 6983 | hg19 | 6983 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13863658, essv13863650, essv13863653, essv13863656, essv13863652, essv13863657, essv13863661, essv13863648, essv13863660, essv13863654, essv13863649, essv13863659, essv13863655, essv13863651 | Samples | HG04210, HG02017, HG03490, HG03765, NA20795, HG03905, HG03884, NA12748, HG03643, NA18541, HG01444, NA20792, NA19785, HG01082 | Known Genes | ADK | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623834
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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