Variant DetailsVariant: dgv5147n223| Internal ID | 22808115 | | Landmark | | | Location Information | | | Cytoband | 4p16.1 | | Allele length | | Assembly | Allele length | | hg38 | 38532 | | hg19 | 38532 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nsv6373734, nsv6364032, nsv6362505 | | Samples | | | Known Genes | LOC650293 | | Method | Sequencing | | Analysis | | | Platform | | | Comments | | | Reference | Sedlazeck_et_al_2020 | | Pubmed ID | 99999999 | | Accession Number(s) | dgv5147n223
| | Frequency | | Sample Size | 19652 | | Observed Gain | 0 | | Observed Loss | 3 | | Observed Complex | 0 | | Frequency | n/a |
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