Variant DetailsVariant: nsv1137631Internal ID | 18926844 | Landmark | | Location Information | | Cytoband | 9p13.1 | Allele length | Assembly | Allele length | hg38 | 179701 | hg19 | 179701 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3990132 | Samples | KWS2 | Known Genes | CNTNAP3, SPATA31A1, SPATA31A2 | Method | Sequencing | Analysis | HugeSeq | Platform | Illumina HiSeq 2000 | Comments | | Reference | Alsmadi_et_al_2014 | Pubmed ID | 24896259 | Accession Number(s) | nsv1137631
| Frequency | Sample Size | 2 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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