Variant DetailsVariant: nsv972950Internal ID | 18261480 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 121905 | hg19 | 121905 | hg18 | 121905 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2766459, nssv2762252, nssv2760037, nssv2758638, nssv2757806, nssv2759222 | Samples | HGDP00665, HGDP00998, HGDP00778, HGDP01307, HGDP00542, HGDP00927 | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv972950
| Frequency | Sample Size | 10 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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