Variant DetailsVariant: esv2657875Internal ID | 9577294 | Landmark | | Location Information | | Cytoband | 7p22.1 | Allele length | Assembly | Allele length | hg38 | 24548 | hg19 | 24548 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1183e199 | Supporting Variants | essv5594304, essv5770145, essv5952231, essv6067052, essv6596954, essv5493105, essv5845270, essv6039307, essv5928265, essv5702549, essv6240588, essv6378322, essv5859411, essv5869002, essv6098482, essv6257023, essv5512782, essv5936870, essv6560631, essv5814723 | Samples | NA19204, NA18486, NA18504, NA19190, NA18510, NA19107, NA18916, NA19197, NA19235, NA18520, NA18867, NA18934, NA18516, NA18499, NA18856, NA18853, NA19257, NA19108, NA19248, NA19129 | Known Genes | USP42 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2657875
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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