Variant DetailsVariant: esv2666630Internal ID | 9586049 | Landmark | | Location Information | | Cytoband | 9q22.2 | Allele length | Assembly | Allele length | hg38 | 84 | hg19 | 84 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6116353, essv6493582, essv6385123, essv5667942, essv5716239, essv6232116, essv5663180 | Samples | NA19394, NA18504, NA19381, NA19379, NA19428, NA19398, NA19093 | Known Genes | LOC100129316 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2666630
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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