Variant DetailsVariant: esv2660206Internal ID | 9579625 | Landmark | | Location Information | | Cytoband | 17p13.2 | Allele length | Assembly | Allele length | hg38 | 840248 | hg19 | 840248 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5914054 | Samples | NA18574 | Known Genes | ASPA, CLUH, MIR1253, MIR6776, OR1A1, OR1A2, OR1D2, OR1D4, OR1D5, OR1E1, OR1E2, OR1G1, OR3A1, OR3A2, OR3A3, OR3A4P, PAFAH1B1, RAP1GAP2, SPATA22, TRPV3 | 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) | esv2660206
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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