Variant DetailsVariant: esv2660203Internal ID | 9579622 | Landmark | | Location Information | | Cytoband | 16p13.2 | Allele length | Assembly | Allele length | hg38 | 1677 | hg19 | 1677 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5399102, essv6427926, essv5408178, essv6308600, essv5487094, essv5929295, essv6537532, essv6259730, essv6108170, essv5726295, essv5726082, essv6060533, essv5929901, essv5973827, essv5548263, essv5612323, essv6226094 | Samples | NA19350, NA18486, NA20294, NA18510, NA19904, NA19901, NA19189, NA18520, NA19908, NA19461, NA20282, NA19452, NA18517, NA19380, NA19311, NA19711, NA20322 | Known Genes | ABAT | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660203
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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