Variant DetailsVariant: esv3891986Internal ID | 18839696 | Landmark | | Location Information | | Cytoband | 11p11.12 | Allele length | Assembly | Allele length | hg38 | 1261306 | hg19 | 1261306 | hg18 | 1261306 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25788268 | Samples | | Known Genes | FOLH1, OR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ, TRIM49B, TRIM64C | Method | SNP array | Analysis | | Platform | Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891986
| Frequency | Sample Size | 3017 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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