Variant DetailsVariant: nsv554811Internal ID | 15995534 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 87215 | hg19 | 87215 | hg18 | 87215 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1906n54 | Supporting Variants | nssv1174650, nssv775178, nssv775177, nssv1174651, nssv775173, nssv775174, nssv775175, nssv1174653, nssv1174652, nssv1174649, nssv775172, nssv1174654, nssv775176 | Samples | HGDP00791, HGDP00881, NINDS_247, HGDP00520, HGDP01021, NINDS_256 | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv554811
| Frequency | Sample Size | 17421 | Observed Gain | 7 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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