Variant DetailsVariant: nsv950784Internal ID | 16952971 | Landmark | | Location Information | | Cytoband | 7p22.3 | Allele length | Assembly | Allele length | hg38 | 218701 | hg19 | 218700 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2997588 | Samples | BILGI_BIOE | Known Genes | ADAP1, C7orf50, COX19, CYP2W1, GET4, GPR146, MIR339, SUN1 | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nsv950784
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|