<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE alias="S13-1" accession="SRS1871917">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS1871917</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN06065503</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">1247-S13-1</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs001247" label="submitted sample id">S13-1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Non-tumor DNA sample from Blood of a human female participant in the dbGaP study "GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs001247</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>NCI GMKF Cranial Dysinnervation Disorders</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>NCI GMKF Cranial Dysinnervation Disorders</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Family/Twin/Trios</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>S13-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>S13-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>13-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>2172067</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>1800842</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Cranial Nerve Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>histological type</TAG>
        <VALUE>Lymphocyte</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>is tumor</TAG>
        <VALUE>No</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP/CNV Genotypes (NGS)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>3</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>DS-CCDD-RD</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
</SAMPLE_SET>
