Variant DetailsVariant: nssv1148372Internal ID | 15654872 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 127707 | hg19 | 127707 | hg18 | 127707 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv616017 | Supporting Variants | | Samples | | Known Genes | C9orf169, C9orf173, EXD3, FAM166A, LOC100129722, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, TMEM203, TOR4A, TPRN, TUBB4B | 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) | nssv1148372
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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