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Table 3 List of variants of uncertain significance

From: Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong

Patient number Gender/group Array CGH result [hg18] Chromosome region Aberration type Size (Mb) IQ Additional clinical features
9 Male/adult arr 3q13.3 (111,747,166–112,297,084) × 3 3q13.3 Duplication 0.55 96 Nil
10 Male/adult arr 1q44 (244,474,644–245,087,421) × 3 1q44 Duplication 0.61 85 Nil
11 Female/adult arr 11q24.1 (122,330,312–122,406,276) × 3 11q24.1 Duplication 0.08 103 Nil
12 Female/paediatric arr 10p12.33p12.32 (19,502,326–20,471,711) × 3 10p12.33–p12.32 Duplication 0.97 N/A Scoliosis
13 Male/paediatric arr 17q21.33 (45,861,307–45,986,282) × 3 17q21.33 Duplication 0.12 N/A Developmental delay
14 Male/paediatric arr 6q14.1 (82,900,869–83,543,710) × 3 6q14.1 Duplication 0.64 N/A Developmental delay/regression, asthma, severe eczema
15 Male/paediatric arr 5q33.1 (148,226,533–148,809,596) × 1 5q33.1 Deletion 0.58 N/A Nil
  1. N/A not available