Variant DetailsVariant: dgv13006n54Internal ID | 20146430 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 106774 | hg19 | 106774 | hg18 | 106774 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv615978, nsv615981 | Samples | 1780862388_A, 1780862100_A | Known Genes | AGPAT2, EGFL7, FAM69B, MIR126, SNHG7 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | dgv13006n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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