Variant DetailsVariant: nsv545916Internal ID | 15986639 | Landmark | | Location Information | | Cytoband | 1p35.3 | Allele length | Assembly | Allele length | hg38 | 415629 | hg19 | 415630 | hg18 | 415630 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv712049 | Samples | | Known Genes | ATPIF1, DNAJC8, MED18, PHACTR4, RAB42, RCC1, SESN2, SNHG12, SNHG3, SNORA16A, SNORA44, SNORA61, SNORD99, TAF12, TRNAU1AP | 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) | nsv545916
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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