Variant DetailsVariant: dgv3290n106Internal ID | 20162647 | Landmark | | Location Information | | Cytoband | 6p22.3 | Allele length | Assembly | Allele length | hg38 | 6116 | hg19 | 6116 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1120883, nsv1112120 | Samples | KWS2, KWS1 | Known Genes | FAM65B | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Alsmadi_et_al_2014 | Pubmed ID | 24896259 | Accession Number(s) | dgv3290n106
| Frequency | Sample Size | 2 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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