View CNVs/SVs
View by Evidence Type: Significant Enriched CNVs (
CNVs Only Present In Patients
de novo CNVs
Overlapping/Recurrent CNVs
CNVs Overlapping With ACRD
CNVs Not Present In Control
Significant Enriched CNVs
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View by Chromosome:15 ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y All )
Notes: ACRD: Autism Chromosome Rearrangement Database
CNV Name | Chr | Band | Gain/Loss | Number of CNVs | Evidence Type | Reference | |
---|---|---|---|---|---|---|---|
Case | Control | ||||||
AutCNV0000368 | 15 | 15q21.1 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Zwaag, 2009 |
AutCNV0004964 | 15 | 15q12 | gain | 28 | 0 | CNVs Only Present In Patients; Significant Enriched CNVs; | Hadley D, 2014 |
AutCNV0004965 | 15 | 15q12 | gain | 27 | 1 | CNVs Only Present In Patients; Significant Enriched CNVs; | Hadley D, 2014 |
AutCNV0004966 | 15 | 15q13.1 | gain | 24 | 0 | CNVs Only Present In Patients; Significant Enriched CNVs; | Hadley D, 2014 |
AutCNV0004979 | 15 | 15q11.2-13.1 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; | Sanders SJ, 2015 |
AutCNV0004980 | 15 | 15q12 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; | Sanders SJ, 2015 |
AutCNV0004981 | 15 | 15q13.2-13.3 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; | Sanders SJ, 2015 |
AutCNV0005080 | 15 | 15q11.2 | loss | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Siu WK, 2016 |
AutCNV0005081 | 15 | 15q23q24.1 | loss | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Siu WK, 2016 |
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