Variant DetailsVariant: nsv1140249Internal ID | 18936662 | Landmark | | Location Information | | Cytoband | 19p12 | Allele length | Assembly | Allele length | hg38 | 171726 | hg19 | 171726 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3978962 | Samples | KWS2 | Known Genes | ZNF493, ZNF708, ZNF738 | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Alsmadi_et_al_2014 | Pubmed ID | 24896259 | Accession Number(s) | nsv1140249
| Frequency | Sample Size | 2 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|