Variant DetailsVariant: esv2659526Internal ID | 9578945 | Landmark | | Location Information | | Cytoband | 13q14.13 | Allele length | Assembly | Allele length | hg38 | 1565 | hg19 | 1565 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5485715, essv6431976, essv5851200, essv6200588, essv6355951, essv5555722, essv6299579, essv6171499, essv6215392, essv5942115 | Samples | NA18980, NA18599, HG00640, NA19057, NA19381, NA19075, HG00118, HG00613, HG00111, HG01125 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2659526
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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