Variant DetailsVariant: essv25792934Internal ID | 18819777 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 147008 | hg19 | 147008 | hg18 | 147008 |
| Variant Type | CNV gain | Copy Number | 3 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3892883 | Supporting Variants | | Samples | | Known Genes | COG4, IL34, SF3B3, SNORD111, SNORD111B | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | Number of probes=21 | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | essv25792934
| Frequency | Sample Size | 3017 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|