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7q31.33-q32.3CNV Type: Deletion


Largest CNV size: 5799214 bp

Statistics Box:
Number of Reports: 2



Summary Information

Rare singleton deletion within this region was found in a case from a study of 15,749 individuals from the International Standards for Cytogenomic Arrays (ISCA) consortium with unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome (Kaminsky et al., 2011).

Additional Locus Information

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References

Major Reports

Title
Author, Year
Report Class
CNV Type
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Deletion

Minor Reports

Title
Author, Year
Report Class
CNV Type
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
Deletion

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 kaminsky_11_DD/ID/ASD_discovery_cases
 Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
 15749
 Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
 NA
 NA
 5799214
 1
 0
 1
 mahjani_21_ASD_discovery_cases
 Study participants in the PAGES cohort, a large ongoing population-based cohort study in Sweden that started in 2012 with the overall aim to identify possible genetic and environmental risk factors for ASD.
 996
 Cases diagnosed with ASD according to ICD-9 and ICD-10 criteria.
 Average age at diagnosis, 8.2 yrs.
 70% Male
 7685970
 1
 0
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 kaminsky_11_DD/ID/ASD_discovery_controls
 Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
 10118
 Controls
 NA
 NA
 NA
 NA
 NA
 NA

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 kaminsky_11_DD/ID/ASD_discovery_cases
  NA
 aCGH
  Agilent 44K, Agilent 105K
 
 Feature Extraction, DNA Analytics
 FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
 mahjani_21_ASD_discovery_cases
  Sweden
 WES
  Infinium OmniExpress Exome
 PennCNV
 NA
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  kaminsky_11_DD/ID/ASD_discovery_controls
  NA
  aCGH
  Agilent 44K, Agilent 105K
 
  Feature Extraction, DNA Analytics
 

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004284
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 126859732
 132750936
  5891205
 GRCh38
 Deletion
 Yes
  mahjani_21_ASD_discovery_cases-case215
 NA
 M
 ASD
 Diagnosis of ASD according to ICD-9 and ICD-10 criteria.
 
 124821802
 132507771
  7685970
 GRCh38
 Deletion
 No

Controls

No Control Data Available

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004284
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 De novo
 Unknown
 Unknown
 MIR592,PRELID3BP10,ARF5,SND1-IT1,LRRC4,MIR593,MIR129-1,RNU7-27P,RNU7-54P,HILPDA,RNU6-177P,CICP14,IMP3P2,RNA5SP242,RNA5SP243,RN7SL81P,OPN1SW,ATP6V1F,ATP6V1FNB,RN7SL306P,ODCP,CYCSP20,RNY1P11,SNRPGP3,RNU1-72P,SMKR1,RNA5SP244,MIR182,MIR96,MIR183,RNA5SP245,SSMEM1,MESTIT1,MIR335,RNA5SP246,KLF14,MIR29A,MIR29B1,RNU6-1010P,EEF1B2P6,NDUFB9P2,GCC1,FSCN3,PAX4,LEP,PRRT4,IMPDH1,METTL2B,FAM71F2,CALU,CCDC136,FLNC-AS1,KCP,IRF5,TPI1P2,TSPAN33,SMO,STRIP2,KLHDC10,TMEM209,CPA4,CPA5,CPA1,MEST,LINC00513,LINC-PINT,MKLN1-AS,PODXL,FLJ40288,ZNF800,RBM28,FAM71F1,FLNC,AHCYL2,NRF1,UBE2H,CPA2,CEP41,COPG2,TSGA13,MKLN1,PLXNA4,GRM8,SND1,TNPO3,ZC3HC1
 
 mahjani_21_ASD_discovery_cases-case215
 
 
 Unknown
 
 
 ARF5,OPN1SW,CALU,FLNC,CPA2,CPA1,COPG2,SND1,SND1-IT1,CPA4,FSCN3,HILPDA,ZC3HC1,RBM28,COPG2IT1,STRIP2,METTL2B,CCDC136,GCC1,LRRC4,TMEM209,PLXNA4,CPA5,CEP41,TSGA13,SSMEM1,KLF14,ZNF800,IMPDH1,IRF5,GRM8,MESTIT1,TSPAN33,TPI1P2,CYCSP20,LINC-PINT,KCP,MIR29A,PRRT4,MIR182,MIR129-1,POT1-AS1,MIR96,MIR29B1,MIR183,MIR335,EEF1B2P6,EEF1GP1,PRELID3BP10,MIR592,MIR593,CDC26P1,NDUFB9P2,CICP14,ATP6V1FNB,CAPZA1P4,NRF1,MEST,ODCP,PAX4,LEP,MKLN1,RNU7-27P,RNU7-54P,SMKR1,LINC00513,MKLN1-AS,RNA5SP242,RNA5SP245,RNA5SP246,RNA5SP244,SNRPGP3,PODXL,GRM8-AS1,LINC02830,RNA5SP243,RN7SL81P,UBE2H,SMO,IMP3P2,RNU6-177P,RN7SL306P,RNU6-1010P,RNY1P11,RNU1-72P,FLNC-AS1,H4P1,PPIAP93,ATP6V1F,KLHDC10,AHCYL2,TNPO3,POT1
 

Controls

No Control Data Available
No Animal Model Data Available
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