Variant DetailsVariant: nsv555226Internal ID | 15995949 | Landmark | | Location Information | | Cytoband | 11q13.1 | Allele length | Assembly | Allele length | hg38 | 265791 | hg19 | 265791 | hg18 | 265791 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv778085 | Samples | | Known Genes | C11orf80, C11orf86, LRFN4, MIR6860, PC, RCE1, RHOD, SYT12 | 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) | nsv555226
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|