Variant DetailsVariant: nsv562886Internal ID | 16003609 | Landmark | | Location Information | | Cytoband | 13q32.2 | Allele length | Assembly | Allele length | hg38 | 908 | hg19 | 908 | hg18 | 908 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3349n54 | Supporting Variants | nssv817806, nssv817803, nssv817807, nssv817802, nssv817804, nssv817805, nssv817808 | Samples | | Known Genes | STK24 | 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) | nsv562886
| Frequency | Sample Size | 17421 | Observed Gain | 3 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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