Variant DetailsVariant: nssv851741Internal ID | 15799011 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 165136 | hg19 | 165136 | hg18 | 165136 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv571012 | Supporting Variants | | Samples | | Known Genes | C16orf13, CCDC78, FAM173A, FAM195A, FBXL16, HAGHL, JMJD8, METRN, NARFL, PIGQ, RAB40C, RHBDL1, RHOT2, STUB1, WDR24, WDR90, WFIKKN1 | 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) | nssv851741
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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