Variant DetailsVariant: nsv1141278Internal ID | 18939923 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 136501 | hg19 | 136501 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3992784 | Samples | KWS2 | Known Genes | LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1 | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Alsmadi_et_al_2014 | Pubmed ID | 24896259 | Accession Number(s) | nsv1141278
| Frequency | Sample Size | 2 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|