Variant DetailsVariant: esv3636621Internal ID | 6676728 | Landmark | | Location Information | | Cytoband | 15q21.3 | Allele length | Assembly | Allele length | hg38 | 30117 | hg19 | 30117 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15260043, essv15260041, essv15260044, essv15260042 | Samples | HG02784, HG03018, NA18962, NA18537 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3636621
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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