Variant DetailsVariant: esv2661207Internal ID | 9580626 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 24842 | hg19 | 24848 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv135e199 | Supporting Variants | essv5961165, essv5402541, essv5782902, essv5661305, essv6025534, essv6222589, essv5910623, essv5488554, essv6410997, essv5628535, essv6170458, essv5879948, essv6305543, essv5949203, essv5994073, essv6304340, essv6086320, essv6453377, essv6047991, essv5562360 | Samples | NA19664, NA19777, NA19684, NA19728, NA19678, NA19723, NA19782, NA19720, NA19651, NA19719, NA19725, NA19717, NA19788, NA19750, NA19675, NA19679, NA19786, NA19783, NA19716, NA19676 | Known Genes | ANXA8L1, ANXA8L2, FAM25B | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661207
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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