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Table 4 Details of samples with discordant array and NIPT CNV results

From: Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray

Sample ID

Array result

Diagnostic procedure

Fetal fraction

cfDNA reported result

uni/biplex result

45164

7p22.3p15.2(43,360–26,275,617) × 3, 7p15.2(26,275,995–26,341,643) × 1, 15q26.2q26.3(98,178,487–102,429,112) × 1

Amnio

0.125

Negative

del15q26.2q26.3

76383

15q21.2q26.3 (50,945,434–102,531,392) × 3

Amnio

0.080

Negative

Negative

45287

arr(1–22,X) × 2

CVS

0.109

45,X

45,X

40681

arr(1–22,X) × 2

Amnio

0.089

47,XXX

(suspected maternal)

NA

77361

arr(1–22,X) × 2

Amnio

0.046

47,XXX

(suspected maternal)

NA

76393

arr(1–22,X) × 2

Amnio

0.049

del15q11.2-q13.1

Negative

94767

arr(1–22) × 2,(XY) × 1

Amnio

0.054

del5p15

Negative

76177

arr(1–22) × 2,(XY) × 1

Amnio

0.095

T13 (mosaic)

T13 (mosaic)

93941

arr(1–22,X) × 2

Amnio

0.045

T14

T14 (mosaic)

76354

arr(1–22) × 2,(XY) × 1

Amnio

0.125

T16

T16

76178

arr(1–22,X) × 2

Amnio

0.068

T16

T16

94932

arr(1–22,X) × 2

Amnio

0.169

T16

T16

76028

arr(1–22) × 2,(XY) × 1

Amnio

0.095

T16 (mosaic)

T16 (mosaic)

54712

arr(1–22,X) × 2

Amnio

0.102

T21 (mosaic)

T21 (mosaic)

54705

arr(1–22) × 2,(XY) × 1

CVS

0.077

T22 (mosaic)

Failed re-sequencing

82511

arr(1–22,X) × 2

Amnio

0.176

T7

T7

94639

arr(1–22,X) × 2

Amnio

0.124

T7 (mosaic)

T7

94666

arr(1–22,X) × 2

Amnio

0.108

T7 (mosaic)

T7 (mosaic)

40637

arr(1–22) × 2,(XY) × 1

Amnio

0.118

T7/T21 (mosaic)

T7/T21 (mosaic)

  1. cfDNA cell-free DNA, NA not applicable, CVS chorionic villus sampling, T13 trisomy 13, T14 trisomy 14, T16 trisomy 16, T21 trisomy 21, T22 trisomy 22, T7 trisomy 7