Variant DetailsVariant: esv2746942Internal ID | 9981226 | Landmark | | Location Information | | Cytoband | 12q24.33 | Allele length | Assembly | Allele length | hg38 | 541 | hg19 | 541 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6940452, essv6846030, essv6687966, essv6688371, essv6894749, essv6831403, essv6891368, essv6924455 | Samples | SSM097, SSM018, SSM035, SSM085, SSM081, SSM005, SSM022, SSM098 | Known Genes | GALNT9 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2746942
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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