Variant DetailsVariant: esv2746532Internal ID | 9980816 | Landmark | | Location Information | | Cytoband | 12q24.31 | Allele length | Assembly | Allele length | hg38 | 609 | hg19 | 609 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6879551, essv6894718, essv6746915, essv6779534, essv6673262, essv6809444, essv6677900, essv6791919, essv6953298, essv6965898, essv6842508, essv6827786, essv6857326, essv6819795, essv6959386, essv6783629, essv6823701 | Samples | SSM027, SSM075, SSM079, SSM087, SSM093, SSM084, SSM026, SSM032, SSM031, SSM067, SSM068, SSM078, SSM080, SSM055, SSM070, SSM025, SSM098 | Known Genes | NCOR2 | 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) | esv2746532
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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