Variant DetailsVariant: nsv951207Internal ID | 16953394 | Landmark | | Location Information | | Cytoband | 9q34.3 | Allele length | Assembly | Allele length | hg38 | 242200 | hg19 | 242200 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2997043 | Samples | BILGI_BIOE | Known Genes | ANAPC2, C9orf169, C9orf173, EXD3, FAM166A, GRIN1, LOC100129722, LRRC26, MIR3621, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, SSNA1, TMEM203, TMEM210, TOR4A, TPRN, TUBB4B | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nsv951207
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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