Variant DetailsVariant: esv2666228Internal ID | 9585647 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 201 | hg19 | 201 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5852175, essv6092436, essv6465751, essv6371983, essv6350983, essv6125955, essv6153949, essv5582106 | Samples | NA11830, HG01173, HG00337, HG00185, HG01080, HG00323, HG00282, NA20754 | Known Genes | ADARB2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2666228
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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