Variant DetailsVariant: esv2669637Internal ID | 9589056 | Landmark | | Location Information | | Cytoband | 14q12 | Allele length | Assembly | Allele length | hg38 | 44012 | hg19 | 44012 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6563684 | Samples | HG00320 | Known Genes | CIDEB, DHRS1, LTB4R, LTB4R2, NOP9 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2669637
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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