Variant DetailsVariant: dgv8516n54| Internal ID | 22776411 | | Landmark | | | Location Information | | | Cytoband | 3q13.32 | | Allele length | | Assembly | Allele length | | hg38 | 72741 | | hg19 | 72741 | | hg18 | 72741 |
| | Variant Type | CNV gain | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nsv591359, nsv591351 | | Samples | | | Known Genes | IGSF11 | | 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) | dgv8516n54
| | Frequency | | Sample Size | 17421 | | Observed Gain | 3 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
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