Variant DetailsVariant: dgv3964n54Internal ID | 20137388 | Landmark | | Location Information | | Cytoband | 14q32.33 | Allele length | Assembly | Allele length | hg38 | 2955 | hg19 | 2955 | hg18 | 2955 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv566106, nsv566108, nsv566100, nsv566104, nsv566102, nsv566107 | Samples | | Known Genes | CEP170B | 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) | dgv3964n54
| Frequency | Sample Size | 17421 | Observed Gain | 14 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|