Variant DetailsVariant: nssv3000017Internal ID | 16946283 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 419299 | hg19 | 419300 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv953306 | Supporting Variants | | Samples | BILGI_BIOE | Known Genes | ARFGAP1, BIRC7, C20orf195, CHRNA4, COL20A1, EEF1A2, FLJ16779, HELZ2, KCNQ2, MIR124-3, MIR3196, MIR4326, NKAIN4, PPDPF, PTK6, SRMS, YTHDF1 | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nssv3000017
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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