Variant DetailsVariant: nsv560956Internal ID | 16001679 | Landmark | | Location Information | | Cytoband | 12q24.33 | Allele length | Assembly | Allele length | hg38 | 1662 | hg19 | 1662 | hg18 | 1662 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3017n54 | Supporting Variants | nssv805494, nssv805491, nssv805490, nssv805489, nssv805492, nssv805497, nssv805496, nssv805493, nssv805495 | Samples | | Known Genes | NOC4L | 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) | nsv560956
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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