Variant DetailsVariant: essv25797567Internal ID | 18827517 | Landmark | | Location Information | | Cytoband | 2q21.1 | Allele length | Assembly | Allele length | hg38 | 214721 | hg19 | 214721 | hg18 | 214721 |
| Variant Type | CNV loss | Copy Number | 1 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3893359 | Supporting Variants | | Samples | | Known Genes | CCDC74A, LINC01120, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D, WTH3DI | Method | SNP array | Analysis | | Platform | Illumina Human OmniExpress | Comments | Number of probes=24 | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | essv25797567
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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