Variant DetailsVariant: dgv1178n100Internal ID | 20152794 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 101794 | hg19 | 101794 | hg18 | 101794 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1037738, nsv1036981, nsv1053378, nsv1042485, nsv1046927, nsv1045061 | Samples | | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv1178n100
| Frequency | Sample Size | 29084 | Observed Gain | 8 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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