Variant DetailsVariant: nsv952596Internal ID | 16954783 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 15100 | hg19 | 15100 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2999063 | Samples | BILGI_BIOE | Known Genes | CHRFAM7A, LOC101059918 | Method | Sequencing | Analysis | | Platform | Illumina HiSeq 2000 | Comments | | Reference | Dogan_et_al_2014 | Pubmed ID | 24416366 | Accession Number(s) | nsv952596
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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