Variant DetailsVariant: nsv616007Internal ID | 16056730 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 161299 | hg19 | 161299 | hg18 | 161299 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1148361 | Samples | | Known Genes | ANAPC2, C9orf169, DPP7, GRIN1, LRRC26, MAN1B1, MAN1B1-AS1, MIR3621, NDOR1, RNF208, RNF224, SLC34A3, SSNA1, TMEM203, TMEM210, TPRN, UAP1L1 | 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) | nsv616007
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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