Variant DetailsVariant: esv3621931Internal ID | 6662107 | Landmark | | Location Information | | Cytoband | 9q34.2 | Allele length | Assembly | Allele length | hg38 | 17448 | hg19 | 17448 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13638926, essv13638924, essv13638927, essv13638916, essv13638917, essv13638921, essv13638920, essv13638925, essv13638923, essv13638922, essv13638919, essv13638918, essv13638928 | Samples | HG02150, HG04002, HG04018, NA18627, HG02595, HG00260, HG03428, HG03969, HG00476, HG01108, HG01804, HG03410, HG02406 | Known Genes | CEL | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3621931
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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