Variant DetailsVariant: nsv555174Internal ID | 15995897 | Landmark | | Location Information | | Cytoband | 11q12.3 | Allele length | Assembly | Allele length | hg38 | 162424 | hg19 | 162424 | hg18 | 162424 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv777139 | Samples | | Known Genes | B3GAT3, BSCL2, C11orf48, C11orf83, EEF1G, EML3, GANAB, GNG3, HNRNPUL2, HNRNPUL2-BSCL2, INTS5, LOC102288414, LRRN4CL, METTL12, MIR6747, MTA2, ROM1, SNORA57, TTC9C, TUT1, UBXN1 | 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) | nsv555174
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|