Variant DetailsVariant: dgv4428n54Internal ID | 20137852 | Landmark | | Location Information | | Cytoband | 15q13.3 | Allele length | Assembly | Allele length | hg38 | 38113 | hg19 | 38113 | hg18 | 38113 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv568769, nsv568768, nsv568771, nsv568770 | Samples | 1780854419_A | Known Genes | MIR211, TRPM1 | 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) | dgv4428n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
|
|