Variant DetailsVariant: esv2728570Internal ID | 9962884 | Landmark | | Location Information | | Cytoband | 4q32.1 | Allele length | Assembly | Allele length | hg38 | 983 | hg19 | 983 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6974058, essv6825995, essv6690087, essv6739626, essv6683647, essv6798454, essv6756898, essv6918358, essv6670486, essv6930057, essv6829817, essv6956336, essv6938604, essv6848512, essv6700622, essv6693771, essv6922698, essv6790124 | Samples | SSM036, SSM008, SSM039, SSM018, SSM029, SSM026, SSM017, SSM031, SSM086, SSM081, SSM072, SSM020, SSM080, SSM037, SSM022, SSM070, SSM034, SSM052 | Known Genes | ASIC5 | 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) | esv2728570
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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