Variant DetailsVariant: esv2670824Internal ID | 9590243 | Landmark | | Location Information | | Cytoband | 2q21.1 | Allele length | Assembly | Allele length | hg38 | 979955 | hg19 | 979955 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5502477, essv5863215 | Samples | NA19088, HG01067 | Known Genes | AMER3, ARHGEF4, CCDC74A, CYP4F30P, FAM168B, GPR148, LINC01120, LOC150776, LOC401010, LOC440910, MIR4784, MZT2A, PLEKHB2, POTEE, POTEJ, POTEKP, RNU6-81P, TUBA3D, WTH3DI | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2670824
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
|
|