Variant DetailsVariant: esv2668617Internal ID | 9588036 | Landmark | | Location Information | | Cytoband | 9q22.32 | Allele length | Assembly | Allele length | hg38 | 460 | hg19 | 460 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5872233, essv6286199, essv6121266, essv6084566, essv6579139, essv5943030 | Samples | HG00231, HG00242, HG01066, HG00244, HG00173, HG00326 | Known Genes | FBP1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2668617
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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