Variant DetailsVariant: esv3893457Internal ID | 18837591 | Landmark | | Location Information | | Cytoband | 22q11.22 | Allele length | Assembly | Allele length | hg38 | 1338318 | hg19 | 1338042 | hg18 | 1338042 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25793050 | Samples | | Known Genes | BCR, C22orf15, C22orf43, CES5AP1, CHCHD10, DDT, DDTL, DERL3, FBXW4P1, GNAZ, GSTT2, GSTT2B, GUSBP11, IGLL1, IGLL5, LOC284889, MIF, MIR650, MMP11, RAB36, RGL4, RTDR1, SLC2A11, SMARCB1, VPREB3, ZDHHC8P1, ZNF70 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 550 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3893457
| Frequency | Sample Size | 3017 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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