Variant DetailsVariant: nsv555225Internal ID | 15995948 | Landmark | | Location Information | | Cytoband | 11q13.1 | Allele length | Assembly | Allele length | hg38 | 165929 | hg19 | 165929 | hg18 | 165929 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1174658 | Samples | 1782681216_A | Known Genes | C11orf80, LRFN4, PC, RCE1, SPTBN2 | 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) | nsv555225
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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