Variant DetailsVariant: nssv3768783Internal ID | 18962391 | Landmark | | Location Information | | Cytoband | 7p22.3 | Allele length | Assembly | Allele length | hg38 | 1602 | hg19 | 1602 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv1074045 | Supporting Variants | | Samples | KWP1 | Known Genes | FAM20C | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Thareja_et_al_2015 | Pubmed ID | 25765185 | Accession Number(s) | nssv3768783
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|