Variant DetailsVariant: esv3891151Internal ID | 18838861 | Landmark | | Location Information | | Cytoband | 7q21.11 | Allele length | Assembly | Allele length | hg38 | 23020 | hg19 | 23020 | hg18 | 23020 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25797250, essv25797459, essv25797658, essv25797852, essv25797400, essv25798085, essv25796520, essv25797705, essv25796067, essv25796170, essv25796818, essv25797276, essv25797905, essv25796228, essv25797786, essv25797506, essv25796390, essv25797270, essv25796863, essv25796552, essv25797262, essv25796523, essv25796444, essv25796608, essv25796316 | Samples | | Known Genes | CD36 | Method | SNP array | Analysis | | Platform | Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891151
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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