Variant DetailsVariant: nsv614156Internal ID | 16054879 | Landmark | | Location Information | | Cytoband | 9p13.3 | Allele length | Assembly | Allele length | hg38 | 90373 | hg19 | 90372 | hg18 | 90372 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv12659n54 | Supporting Variants | nssv1132848 | Samples | | Known Genes | ARID3C, CCL27, CNTFR, CNTFR-AS1, DCTN3, GALT, IL11RA, RPP25L, SIGMAR1 | 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) | nsv614156
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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