Variant DetailsVariant: esv2661565Internal ID | 9580984 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 1924 | hg19 | 1924 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6126860, essv6377184, essv6325945, essv6133094, essv5504461, essv5494979, essv5437903 | Samples | HG01173, NA07347, HG00311, HG00323, NA06989, HG00280, HG00343 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661565
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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