Variant DetailsVariant: esv3644536Internal ID | 6684603 | Landmark | | Location Information | | Cytoband | 19q13.32 | Allele length | Assembly | Allele length | hg38 | 3964 | hg19 | 3964 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16069692, essv16069693, essv16069690, essv16069694, essv16069691 | Samples | NA20896, NA21107, NA21129, NA21086, NA20856 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3644536
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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