Variant DetailsVariant: esv3626731Internal ID | 6666879 | Landmark | | Location Information | | Cytoband | 11q13.2 | Allele length | Assembly | Allele length | hg38 | 981 | hg19 | 981 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14200058, essv14200062, essv14200057, essv14200059, essv14200060, essv14200063, essv14200056, essv14200061 | Samples | HG01802, HG00599, HG02164, HG00560, HG00580, HG01866, HG01862, HG00728 | Known Genes | NDUFS8 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3626731
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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