Variant DetailsVariant: nsv592068Internal ID | 16032791 | Landmark | | Location Information | | Cytoband | 3q25.1 | Allele length | Assembly | Allele length | hg38 | 19009 | hg19 | 19009 | hg18 | 19009 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv8655n54 | Supporting Variants | nssv976843 | Samples | | Known Genes | AADAC, MIR548H2 | 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) | nsv592068
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|