Burden of copy number variation in common variable immunodeficiency.

Common variable immunodeficiency (CVID) has been associated recently with a dramatic increase in total copy number variation burden, the cause of which is unclear. In order to explore further the origin and clinical relevance of this finding, we quantified the total genomic copy number variation (CN...

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Main Authors: Keller, M, Glessner, J, Resnick, E, Perez, E, Chapel, H, Lucas, M, Sullivan, K, Cunningham-Rundles, C, Orange, J, Hakonarson, H
Format: Journal article
Language:English
Published: Blackwell Publishing Ltd 2014
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author Keller, M
Glessner, J
Resnick, E
Perez, E
Chapel, H
Lucas, M
Sullivan, K
Cunningham-Rundles, C
Orange, J
Hakonarson, H
author_facet Keller, M
Glessner, J
Resnick, E
Perez, E
Chapel, H
Lucas, M
Sullivan, K
Cunningham-Rundles, C
Orange, J
Hakonarson, H
author_sort Keller, M
collection OXFORD
description Common variable immunodeficiency (CVID) has been associated recently with a dramatic increase in total copy number variation burden, the cause of which is unclear. In order to explore further the origin and clinical relevance of this finding, we quantified the total genomic copy number variation (CNV) burden in affected patients and evaluated clinical details in relationship to total CNV burden. No correlation was found between total CNV burden and either patient age or time elapsed since symptom onset, and higher total burden did not correlate with incidence of malignancy or other subphenotypes. These findings suggest that the increased CNV burden is static and intrinsic to CVID as a disease.
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spelling oxford-uuid:f9c981cc-e8bd-4d97-9e07-8bc88ac58be82022-03-27T13:00:40ZBurden of copy number variation in common variable immunodeficiency.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f9c981cc-e8bd-4d97-9e07-8bc88ac58be8EnglishSymplectic Elements at OxfordBlackwell Publishing Ltd2014Keller, MGlessner, JResnick, EPerez, EChapel, HLucas, MSullivan, KCunningham-Rundles, COrange, JHakonarson, HCommon variable immunodeficiency (CVID) has been associated recently with a dramatic increase in total copy number variation burden, the cause of which is unclear. In order to explore further the origin and clinical relevance of this finding, we quantified the total genomic copy number variation (CNV) burden in affected patients and evaluated clinical details in relationship to total CNV burden. No correlation was found between total CNV burden and either patient age or time elapsed since symptom onset, and higher total burden did not correlate with incidence of malignancy or other subphenotypes. These findings suggest that the increased CNV burden is static and intrinsic to CVID as a disease.
spellingShingle Keller, M
Glessner, J
Resnick, E
Perez, E
Chapel, H
Lucas, M
Sullivan, K
Cunningham-Rundles, C
Orange, J
Hakonarson, H
Burden of copy number variation in common variable immunodeficiency.
title Burden of copy number variation in common variable immunodeficiency.
title_full Burden of copy number variation in common variable immunodeficiency.
title_fullStr Burden of copy number variation in common variable immunodeficiency.
title_full_unstemmed Burden of copy number variation in common variable immunodeficiency.
title_short Burden of copy number variation in common variable immunodeficiency.
title_sort burden of copy number variation in common variable immunodeficiency
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