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14q22.1-q22.3CNV Type: Deletion


Largest CNV size: 3780000 bp

Statistics Box:
Number of Reports: 1



Summary Information

A de novo deletion within this locus was identified in a male case presenting with moderate developmental delay (Chong et al., 2014).

Additional Locus Information

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USCS Symbol             NCBI Symbol

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            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in...
Deletion

Minor Reports

Title
Author, Year
Report Class
CNV Type

No Minor Reports

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 chong_14_DD/ID/ASD/MCA_discovery_cases
 Patients referred to clinical genetics service and recruited for CMA application study
 105
 Developmental delay/intellectual disability (DD/ID), autism (ASD), and/or multiple congenital anomalies (MCA)
 N/A
 N/A
 3780000
 1
 0
 1

Controls

No Control Data Available

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 chong_14_DD/ID/ASD/MCA_discovery_cases
  Chinese
 aCGH
  High-resolution 180K oligoarray
 
 
 aCGH (NimbleGen)

Controls

No Control Data Available

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  chong_14_DD/ID/ASD/MCA_discovery_cases-caseaCGH1051
 N/A
 M
 Developmental delay
 Moderate developmental delay, multiple congenital anomalies (MCA), dysmorphic features, failure to thrive. Family history: none reported.
 Moderate developmental delay
 51544846
 55320598
  3775753
 GRCh38
 Deletion
 Yes

Controls

No Control Data Available

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 chong_14_DD/ID/ASD/MCA_discovery_cases-caseaCGH1051
 Nimblegen aCGH
 
 De novo
 Simplex (negative family history)
 Segregated
 FRMD6-AS1,RNA5SP385,RNU6-301P,OR7E106P,OR7E159P,COX5AP2,PTGDR,PTGER2,RPS3AP46,MIR5580,ATP5F1CP1,RNU6ATAC9P,MIR4308,FDPSP3,RPSAP13,CHMP4BP1,OR7E105P,RTRAF,LINC02319,TXNDC16,PSMC6,STYX,GNPNAT1,FERMT2,LINC02331,BMP4,CDKN3,CNIH1,GMFB,GCH1,WDHD1,SOCS4,MAPK1IP1L,LGALS3,FRMD6-AS2,FRMD6,GNG2,NID2,GPR137C,ERO1A,DDHD1,SAMD4A,DLGAP5,FBXO34,CGRRF1
 

Controls

No Control Data Available
No Animal Model Data Available
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