Variant DetailsVariant: nsv1068593Internal ID | 18971905 | Landmark | | Location Information | | Cytoband | 1q42.2 | Allele length | Assembly | Allele length | hg38 | 1302 | hg19 | 1302 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3770601 | Samples | KWP1 | Known Genes | FAM89A | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Thareja_et_al_2015 | Pubmed ID | 25765185 | Accession Number(s) | nsv1068593
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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