Variant DetailsVariant: nsv590609Internal ID | 16031332 | Landmark | | Location Information | | Cytoband | 3p13 | Allele length | Assembly | Allele length | hg38 | 1136 | hg19 | 1136 | hg18 | 1136 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv8374n54 | Supporting Variants | nssv965553 | Samples | | Known Genes | EIF4E3, GPR27 | 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) | nsv590609
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|