Variant DetailsVariant: esv3891705Internal ID | 18839415 | Landmark | | Location Information | | Cytoband | 9q31.1 | Allele length | Assembly | Allele length | hg38 | 2269094 | hg19 | 2269094 | hg18 | 2269094 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25797771 | Samples | | Known Genes | ABCA1, FKTN, FSD1L, LOC100996590, LOC286367, MIR8081, NIPSNAP3A, NIPSNAP3B, OR13C2, OR13C3, OR13C4, OR13C5, OR13C8, OR13C9, OR13D1, OR13F1, SLC44A1, TAL2, TMEM38B | Method | SNP array | Analysis | | Platform | Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891705
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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