Variant DetailsVariant: esv2667426Internal ID | 9586845 | Landmark | | Location Information | | Cytoband | 6p22.1 | Allele length | Assembly | Allele length | hg38 | 20581 | hg19 | 20581 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5795737, essv6043089, essv6097428, essv5450150, essv6534603, essv5472586, essv6469021 | Samples | NA20761, NA18635, NA20787, HG00584, NA20581, NA18536, NA19248 | Known Genes | OR12D2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2667426
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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