Variant DetailsVariant: nssv3000013Internal ID | 16946279 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 485904 | hg19 | 542200 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv953302 | Supporting Variants | | Samples | BILGI_BIOE | Known Genes | C20orf166, C20orf166-AS1, CABLES2, COL9A3, GATA5, LAMA5, LINC00659, LOC100127888, MIR1-1, MIR133A2, MRGBP, NTSR1, OGFR, OGFR-AS1, RBBP8NL, RPS21, SLCO4A1 | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nssv3000013
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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