Variant DetailsVariant: dgv516n145| Internal ID | 22813532 | | Landmark | | | Location Information | | | Cytoband | 18q12.1 | | Allele length | | Assembly | Allele length | | hg38 | 2221 | | hg19 | 2221 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nsv3115055, nsv3113943 | | Samples | sample115, sample370, sample235, sample102, sample391, sample89, sample113, sample398 | | Known Genes | | | Method | Oligo aCGH | | Analysis | | | Platform | | | Comments | | | Reference | Lu_et_al_2017 | | Pubmed ID | 28705883 | | Accession Number(s) | dgv516n145
| | Frequency | | Sample Size | 467 | | Observed Gain | 0 | | Observed Loss | 8 | | Observed Complex | 0 | | Frequency | n/a |
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